Wild Hops

Botanical Overview

Wild Hops (Hyptis suaveolens) is a flowering plant in the Lamiaceae family. The traditional uses of this species reflect its genuine medicinal value, validated by generations of practical experience. The mint family (Lamiaceae) includes aromatic herbs and shrubs with square stems, opposite leaves, and two-lipped flowers. Many species produce essential oils in glandular trichomes on their leaves and stems. This family is one of the most important sources of culinary and medicinal herbs worldwide.

General Description

It is generally 1–1. 5 m (3. 3–4. 9 ft) tall, occasionally up to 3 m (9. 8 ft). Stems are hairy, and square in cross section. Leaves are oppositely arranged, 2–10 cm (0. 79–3. 94 in) long, with shallowly toothed margins, and emit a strong minty odor if crushed. Flowers are pink or purple, arranged in clusters of 1–5 in the upper leaf axils.

ⓘ Information
Description adapted from Wikipedia (CC BY-SA 4.0).

Family Context

The Lamiaceae family is large and widely distributed. Notable medicinal members include:

  • Basil — 86 documented uses
  • Rosemary — 60 documented uses
  • Agbo — 54 documented uses
  • Sage — 49 documented uses

Geographic Distribution

Wild Hops has been recorded in 10 countries and territories worldwide, including Benin, Brazil, China, Costa Rica, Indonesia, and others.

Traditional Uses

Wild Hops has been traditionally used for digestive health, respiratory conditions, and pain and inflammation, among other applications.

Digestive health.

  • Carminative
  • Ache(Stomach)
  • Stomachic

For digestive complaints, the herb is typically prepared as a tea or decoction taken before meals. The bitter compounds stimulate digestive secretions and improve nutrient absorption. Some traditions use the powdered root or leaves in small doses as a stomachic tonic.

Respiratory conditions.

  • Catarrh
  • Expectorant
  • Cold

Respiratory conditions are addressed through steam inhalation of the herb’s vapors or internal use as a warm tea. The hot infusion acts as an expectorant, helping to loosen phlegm and clear congestion. Some traditions combine it with honey for coughs.

Pain and inflammation.

  • Ache(Head)

For pain and inflammation, preparations are applied both topically as compresses and taken internally. A warm poultice draws blood to the area and promotes healing, while internal preparations address systemic inflammation.

Active Compounds

Phytochemical research has identified 30 compounds in this species, including a diverse array of phytochemical classes (see the Complete Chemical Inventory below for the full list).

The identified compounds include the following categories:

  • Alkaloid: nitrogenous compounds with diverse pharmacological activities
ⓘ Information
Information on this page is compiled from Dr. Duke’s Phytochemical and Ethnobotanical Databases (USDA ARS), a public domain resource. Consult a healthcare professional before using any herbal preparation.

Distribution and Conservation

Reported distribution: Benin, Brazil, China, Costa Rica, Indonesia, Kenya, Mexico, Senegal, Taiwan, Tanzania.

Complete Use Records

CategoryCultural Context
StimulantElsewhere, Haiti, Malaya, Malaysia, Philippines, Trinidad
CarminativeDominican Republic, Elsewhere, Haiti, Trinidad
CatarrhElsewhere, Malaya, Malaysia
SudorificElsewhere, Malaya, Malaysia
Ache(Stomach)Curacao, Elsewhere
AnalgesicElsewhere, Trinidad
ApertifCuracao, Philippines
DepurativeDominican Republic, Elsewhere
ExpectorantElsewhere, Trinidad
RefrigerantElsewhere, Trinidad
StomachicDominican Republic, Philippines
Ache(Head)India
AntispasmodicElsewhere
BechicDominican Republic
BiliousCuracao
CancerVenezuela
ColdTrinidad
ConstipationTrinidad
DermatosisMalaya
FeverTrinidad
FluTrinidad
GallCuracao
Repellant(Insect)Elsewhere
IntestineMexico
LactagogueJava
LiverCuracao
MalariaTrinidad
MenorrhagiaTrinidad
NauseaCuracao
PacifierCuracao

Complete Chemical Inventory

CompoundFormulaMW
(E)-BETA-OCIMENEC₁₀H₁₆136.23 Da
(Z)-BETA-OCIMENEC₁₀H₁₆136.23 Da
1,1,3-TRIMETHYLDECAHYDROCYCLOPROPAZULENE
1,3,3-TRIMETHYLBICYCLO{2.2.1}-HEPTAN-2-OL
1,4-DIMETHYL,1,2,3,3A,4,5,6,7-OCTAHYDROAZULENE
1,8-CINEOLEC₁₀H₁₈O154.25 Da
2,5-DIMETHYL-3-METHYLENE-1,5-HEPTADIENEC₁₀H₁₆136.23 Da
2,6-DIMETHYL-6-(4-METHYL)BICYCLO{3.1.1}-HEPT-2-ENE
3,7-DIMETHYL-1,6-OCTADIEN-3-OLC₁₀H₁₈O154.25 Da
3-CYCLOHEXEN-1-CARBOXALDEHYDE
4,11,11-TRIMETHYL-8-METHYLENE-BICYCLO{7.2.0}-UNDEC-4-ENE
4-METHYL-1-(1-METHYLETHYL)-3-CYCLOHEXEN-1-OLC₁₀H₁₈O154.25 Da
5ALPHA-ANDROST-2,11-DIONE
5ALPHA-ANDROST-9(11)-EN-12-ONEC₁₉H₂₈O272.4 Da
5BETA,8BETA,H-9BETA,H-10ALPHA-LAB-14-ENE
ALPHA-BERGAMOTENEC₁₅H₂₄204.35 Da
ALPHA-CADINOLC₁₅H₂₆O222.37 Da
ALPHA-CARYOPHYLLENEC₁₅H₂₄204.35 Da
ALPHA-CARYOPHYLLENE-ALCOHOLC₁₅H₂₆O222.37 Da
ALPHA-COPAENEC₁₅H₂₄204.35 Da
ALPHA-CYMENEC₁₀H₁₄134.22 Da
ALPHA-FENCHOLC₁₀H₁₈O154.25 Da
ALPHA-GUAIENEC₁₅H₂₄204.35 Da
ALPHA-HUMULENEC₁₅H₂₄204.35 Da
ALPHA-PHELLANDRENEC₁₀H₁₆136.23 Da
ALPHA-PINENEC₁₀H₁₆136.23 Da
ALPHA-TERPINENEC₁₀H₁₆136.23 Da
ALPHA-TERPINEOLC₁₀H₁₈O154.25 Da
ALPHA-THUJENEC₁₀H₁₆136.23 Da
BETA-BOURBONENEC₁₅H₂₄204.35 Da

Data from PubChem (NIH/NLM, public domain).


References & Further Reading

External Research Links

Data Sources